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B.braun

FDA UDI

Class II (US FDA UDI)

by B. Braun Medical Inc.

Identity

Trade Name
B.BRAUN FDA UDI
Generic Name
Evacuated intravenous fluid container FDA UDI
Device Name
Evacuated IV Container, Glass, 1000 mL FDA UDI
Model / Reference
S9900-10 FDA UDI
Description
Evacuated IV Container, Glass, 1000 mL FDA UDI

Identifiers

Catalog Number
S9900-10 FDA UDI
Primary DI / UDI-DI
04046964187759 FDA UDI
FDA Product Code
KPE FDA UDI
GMDN Term
Evacuated intravenous fluid container FDA UDI

Classification

Device Class
Class II FDA UDI
Regulation Number
880.5025 FDA UDI
Commercial Distribution
In Commercial Distribution FDA UDI

Clinical & Handling

Sterile

Yes

FDA UDI

Single Use

Yes

FDA UDI

Implantable

No

FDA UDI

Contains Latex

No

FDA UDI

Prescription Use

Yes

FDA UDI

Over-the-Counter

No

FDA UDI

Convenience Kit

No

FDA UDI

Combination Product

No

FDA UDI

HCT/P

No

FDA UDI

Premarket Exempt

Yes

FDA UDI

Lot / Batch Number

Yes

FDA UDI

Serial Number

No

FDA UDI

Expiration Date

Yes

FDA UDI

Manufacturing Date

No

FDA UDI

Category: Evacuated intravenous fluid container

B.braun by B. Braun Medical Inc. — Class II — FDA UDI — listed in FDA GUDID — regulatory data on deviCERTS

Similar devices

Also classified as Evacuated intravenous fluid container.

Authorization Coverage (1 country)

Regulatory Authorizations

United States Pending data

FDA UDI

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Manufacturer

Manufacturer
B. Braun Medical Inc.

Sources (1)

  • FDA UDI 7dcbce8c-ba50-49e0-a6ef-5168767fc118 35 fields · synced May 30, 2026